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dc.contributor.authorAkgul S.U.
dc.contributor.authorCinar C.K.
dc.contributor.authorCaliskan Y.
dc.contributor.authorDemir E.
dc.contributor.authorCebeci E.
dc.contributor.authorMeral R.
dc.contributor.authorTemurhan S.
dc.date.accessioned2024-02-04T13:30:04Z
dc.date.available2024-02-04T13:30:04Z
dc.date.issued2023
dc.identifier.issn03011623
dc.identifier.urihttps://doi.org/10.1007/s11255-022-03376-1
dc.identifier.urihttp://hdl.handle.net/11446/4835
dc.description.abstractPurpose: The impact of core 1,3-galactosyltransferase-specific molecular chaperon (COSMC) gene expression and methylation profile on clinical progression of IgA nephropathy (IgAN) is unclear. The aim of this study was to determine the clinical significance and the relation of the COSMC gene expression and methylation pattern with the progression of IgAN. Methods: Thirty-nine biopsy-confirmed IgAN patients, 11 healthy relatives and 20 healthy controls were recruited. The COSMC mRNA levels and methylation profile of COSMC gene promoter were measured using the quantitative real-time PCR. The galactose-deficient IgA1 (Gd-IgA1) levels were measured using ELISA in serum and cell culture supernatant. The effect of IL-4 and AZA on COSMC expression and methylation and the correlation of COSMC gene expression and methylation levels with baseline kidney function tests, histology and long-term outcomes were examined. Results: The mean COSMC mRNA level was significantly lower, and serum Gd-IgA1 level was higher in IgAN patients compared with the control groups (p < 0.001, and p = < 0.001, respectively). The COSMC mRNA levels were correlated with intensity of hematuria (r = ? 0.41, p = 0.009), serum creatinine level (r = ? 0.37, p = 0.002) and eGFR (r = 0.36, p = 0.002). The COSMC methylation levels were correlated with age (r = 0.25, p = 0.04) and baseline eGFR (r = ? 0.326, p = 0.006). Twenty IgAN patients (51.3%) reached to complete (5, 12.8%) or partial remission (15, 38.5%) after a median of 34.5 months (IQR, 13.75–71). In multivariable Cox regression analysis, COSMC mRNA expression (adjusted HR (aHR) 1.871, 95% CI 1.287–2.722, p = 0.001) and Oxford T score (aHR 0.355, 95% CI 0.146–0.859, p = 0.022) predicted the remission. Conclusion: COSMC mRNA level is a novel biomarker candidate to predict the remission in IgAN patients. © 2022, The Author(s), under exclusive licence to Springer Nature B.V.en_US
dc.description.sponsorshipThis Project was supported by the Istanbul University Scientific Research Unit (Project ID:55868).en_US
dc.language.isoengen_US
dc.publisherSpringer Science and Business Media B.V.en_US
dc.relation.ispartofInternational Urology and Nephrologyen_US
dc.identifier.doi10.1007/s11255-022-03376-1
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCore 1,3-galactosyltransferase-specific molecular chaperone (COSMC)en_US
dc.subjectDNA methylationen_US
dc.subjectGalactose-deficient immunoglobulin A1 (Gd-IgA1)en_US
dc.subjectIgA nephropathyen_US
dc.subjectbiological markeren_US
dc.subjectcreatinineen_US
dc.subjectgalactoseen_US
dc.subjectimmunoglobulin A1en_US
dc.subjectimmunoglobulin ANen_US
dc.subjectinterleukin 4en_US
dc.subjectmessenger RNAen_US
dc.subjectunclassified drugen_US
dc.subjectchaperoneen_US
dc.subjectgalactosyl-deficient IgA1en_US
dc.subjectimmunoglobulin Aen_US
dc.subjectmessenger RNAen_US
dc.subjectadulten_US
dc.subjectageen_US
dc.subjectArticleen_US
dc.subjectB lymphocyteen_US
dc.subjectclinical articleen_US
dc.subjectcontrolled studyen_US
dc.subjectCOSMC geneen_US
dc.subjectcreatinine blood levelen_US
dc.subjectdisease associationen_US
dc.subjectdisease exacerbationen_US
dc.subjectDNA methylationen_US
dc.subjectenzyme linked immunosorbent assayen_US
dc.subjectestimated glomerular filtration rateen_US
dc.subjectfemaleen_US
dc.subjectgeneen_US
dc.subjectgene expressionen_US
dc.subjecthematuriaen_US
dc.subjecthistopathologyen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjecthuman tissueen_US
dc.subjectimmunoglobulin A nephropathyen_US
dc.subjectimmunoglobulin blood levelen_US
dc.subjectkidney function testen_US
dc.subjectmaleen_US
dc.subjectoutcome assessmenten_US
dc.subjectpromoter regionen_US
dc.subjectreal time polymerase chain reactionen_US
dc.subjectremissionen_US
dc.subjectscoring systemen_US
dc.subjectgeneticsen_US
dc.subjectimmunoglobulin A nephropathyen_US
dc.subjectmetabolismen_US
dc.subjectGlomerulonephritis, IGAen_US
dc.subjectHumansen_US
dc.subjectImmunoglobulin Aen_US
dc.subjectMolecular Chaperonesen_US
dc.subjectRNA, Messengeren_US
dc.titleCOSMC expression as a predictor of remission in IgA nephropathyen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue4en_US
dc.identifier.volume55en_US
dc.identifier.startpage1033en_US
dc.identifier.endpage1044en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempAkgul, S.U., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey, Transplant Immunology Research Center of Excellence, Koç University, Istanbul, Turkey; Cinar, C.K., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Caliskan, Y., Division of Nephrology, Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, Capa/Fatih, Istanbul, Turkey, Division of Nephrology, Saint Louis University School of Medicine, Saint Louis, MO, United States; Demir, E., Division of Nephrology, Saint Louis University School of Medicine, Saint Louis, MO, United States; Cebeci, E., Department of Nephrology, Health Sciences University, Haseki Training and Research Hospital, Istanbul, Turkey; Meral, R., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Temurhan, S., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Ozluk, Y., Department of Pathology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Aydin, F., Department of Medical Biology and Genetics, Demiroglu Science University, Istanbul, Turkey; Oguz, F.S., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkeyen_US
dc.identifier.pmid36306048en_US
dc.identifier.scopus2-s2.0-85140874898en_US
dc.authorscopusid55668931400
dc.authorscopusid6504219013
dc.authorscopusid55920704400
dc.authorscopusid57192836887
dc.authorscopusid37051798700
dc.authorscopusid57193747679
dc.authorscopusid26031760100


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